Variant report

Variant rs35530977
Chromosome Location chr3:69269711-69269712
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:67 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:69232000-69275600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr3:69242400-69281600 Weak transcription Brain Germinal Matrix brain
3 chr3:69250000-69272400 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr3:69250000-69281600 Weak transcription Esophagus oesophagus
5 chr3:69250200-69286000 Weak transcription Colonic Mucosa Colon
6 chr3:69250400-69280000 Weak transcription Fetal Kidney kidney
7 chr3:69253000-69297600 Weak transcription Gastric stomach
8 chr3:69253400-69277400 Weak transcription Left Ventricle heart
9 chr3:69254000-69280800 Weak transcription Pancreas Pancrea
10 chr3:69254000-69286000 Weak transcription Right Ventricle heart
11 chr3:69254600-69299000 Weak transcription Fetal Brain Male brain
12 chr3:69260000-69285800 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr3:69261000-69269800 Weak transcription Fetal Muscle Leg muscle
14 chr3:69261000-69272800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr3:69261000-69280400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr3:69262200-69274200 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr3:69262400-69276000 Weak transcription Pancreatic Islets Pancreatic Islet
18 chr3:69262600-69286200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
19 chr3:69263000-69273800 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
20 chr3:69263000-69274200 Strong transcription Monocytes-CD14+_RO01746 blood
21 chr3:69263200-69274000 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
22 chr3:69263200-69274200 Strong transcription Dnd41 blood
23 chr3:69263200-69274400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
24 chr3:69263400-69275000 Weak transcription Stomach Mucosa stomach
25 chr3:69263600-69273800 Strong transcription Primary monocytes fromperipheralblood blood
26 chr3:69263600-69275000 Weak transcription Brain Cingulate Gyrus brain
27 chr3:69263800-69270600 Weak transcription HSMMtube muscle
28 chr3:69263800-69275600 Weak transcription Brain Angular Gyrus brain
29 chr3:69263800-69275600 Weak transcription Fetal Muscle Trunk muscle
30 chr3:69263800-69281000 Weak transcription Brain Inferior Temporal Lobe brain
31 chr3:69264000-69270400 Weak transcription Breast Myoepithelial Primary Cells Breast
32 chr3:69264000-69275000 Weak transcription Aorta Aorta
33 chr3:69264600-69275600 Weak transcription Rectal Smooth Muscle rectum
34 chr3:69265200-69272400 Weak transcription Fetal Intestine Small intestine
35 chr3:69265200-69280400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
36 chr3:69265600-69277400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
37 chr3:69266200-69271200 Strong transcription Fetal Heart heart
38 chr3:69266600-69271200 Strong transcription Rectal Mucosa Donor 31 rectum
39 chr3:69266800-69281800 Weak transcription Lung lung
40 chr3:69267000-69273800 Strong transcription Liver Liver
41 chr3:69267200-69273800 Strong transcription Fetal Lung lung
42 chr3:69267600-69270800 Weak transcription HSMM muscle
43 chr3:69268000-69280000 Weak transcription Placenta Placenta
44 chr3:69268400-69271600 Strong transcription Fetal Brain Female brain
45 chr3:69268400-69273200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
46 chr3:69268600-69270000 Strong transcription NHEK skin
47 chr3:69268600-69271200 Strong transcription Rectal Mucosa Donor 29 rectum
48 chr3:69268600-69274000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
49 chr3:69268800-69270000 Strong transcription Primary hematopoietic stem cells short term culture blood
50 chr3:69268800-69270000 Strong transcription Duodenum Smooth Muscle Duodenum

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